Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00226850
Other study ID # 1HUK610
Secondary ID
Status Completed
Phase Phase 3
First received September 12, 2005
Last updated September 23, 2005

Study information

Verified date September 2005
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study examined whether a hypnosis intervention, compared to standard care, could help reduce distress and pain for children undergoing an invasive medical procedure.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 5 Years to 18 Years
Eligibility Inclusion Criteria:

- The child: (1) was scheduled for an upcoming VCUG ; (2) must have undergone at least one previous VCUG; (3) was at least 4 years of age at the time of the previous VCUG; (4) experienced distress during the previous VCUG; and (5) both child and participating parent were English speaking.

Exclusion Criteria:

- Not meeting any of the above criteria.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Behavioral:
hypnosis


Locations

Country Name City State
United States Department of Psychiatry & Behavioral Sciences, Stanford University School of Medicine Stanford California
United States Lucile Packard Children's Hospital Stanford California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

References & Publications (1)

Butler LD, Symons BK, Henderson SL, Shortliffe LD, Spiegel D. Hypnosis reduces distress and duration of an invasive medical procedure for children. Pediatrics. 2005 Jan;115(1):e77-85. — View Citation